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- Q71865336 description "article scientifique publié en 1995" @default.
- Q71865336 description "artículu científicu espublizáu en xunu de 1995" @default.
- Q71865336 description "scientific article published on 01 June 1995" @default.
- Q71865336 description "wetenschappelijk artikel" @default.
- Q71865336 description "наукова стаття, опублікована в червні 1995" @default.
- Q71865336 name "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 name "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 type Item @default.
- Q71865336 label "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 label "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 prefLabel "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 prefLabel "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 P1433 Q71865336-D4272559-3783-4A13-8FF0-0D4A9A2D0751 @default.
- Q71865336 P1476 Q71865336-53279D34-EA5A-48A6-956B-929256B99AFF @default.
- Q71865336 P2093 Q71865336-0482BF78-DA76-480A-8AE2-357739FB33F1 @default.
- Q71865336 P2093 Q71865336-678832E8-C239-43AD-A8DE-20CA3923AD4D @default.
- Q71865336 P2093 Q71865336-6EB0DAE5-EC58-4131-8A32-90E00AEA186D @default.
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- Q71865336 P304 Q71865336-966AAA76-7623-4ABC-86D5-511B54E46B10 @default.
- Q71865336 P31 Q71865336-66A4EE7E-A63E-4D4B-BEBD-B71E401BD007 @default.
- Q71865336 P356 Q71865336-3F447F13-75B5-4E32-9913-B16771E6C39C @default.
- Q71865336 P433 Q71865336-2BF16993-7199-4626-AAD7-CA4D3FA90DD7 @default.
- Q71865336 P478 Q71865336-2554F555-4AFE-49CC-9B23-878E688F2808 @default.
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- Q71865336 P698 Q71865336-8A96CCA3-C147-43F6-9F7D-1536E8D36D4B @default.
- Q71865336 P356 J.1432-1033.1995.0797H.X @default.
- Q71865336 P698 7607254 @default.
- Q71865336 P1433 Q1388041 @default.
- Q71865336 P1476 "Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)" @default.
- Q71865336 P2093 "H Schachter" @default.
- Q71865336 P2093 "J H Charuk" @default.
- Q71865336 P2093 "J Jaeken" @default.
- Q71865336 P2093 "J Tan" @default.
- Q71865336 P2093 "M Bernardini" @default.
- Q71865336 P2093 "R A Reithmeier" @default.
- Q71865336 P2093 "S Haddad" @default.
- Q71865336 P304 "797-805" @default.
- Q71865336 P31 Q13442814 @default.
- Q71865336 P356 "10.1111/J.1432-1033.1995.0797H.X" @default.
- Q71865336 P433 "2" @default.
- Q71865336 P478 "230" @default.
- Q71865336 P577 "1995-06-01T00:00:00Z" @default.
- Q71865336 P698 "7607254" @default.